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Investigating outcome measures for assessing airway clearance techniques in adults with cystic fibrosis: protocol of a single-centre randomised controlled crossover trial
被引:9
|作者:
Stanford, Gemma
[1
,2
]
Davies, Jane C.
[2
,3
]
Usmani, Omar
[2
,4
]
Banya, Winston
[2
,4
]
Charman, Susan
[5
]
Jones, Mandy
[6
]
Simmonds, Nicholas J.
[1
,2
]
Bilton, Diana
[7
]
机构:
[1] Royal Brompton Hosp, Adult Cyst Fibrosis, London, England
[2] Imperial Coll London, Natl Heart & Lung Inst, London, England
[3] Royal Brompton Hosp, Paediat Resp Med, London, England
[4] Royal Brompton Hosp, Res & Dev, London, England
[5] Cyst Fibrosis Trust, London, England
[6] Brunel Univ London, Coll Hlth Med & Life Scientists, Dept Hlth Sci, London, England
[7] Royal Brompton Hosp, Resp Med, London, England
基金:
美国国家卫生研究院;
关键词:
cystic fibrosis;
respiratory measurement;
LUNG-DISEASE;
INDEX;
PHYSIOTHERAPY;
SPIROMETRY;
CHILDREN;
WASHOUT;
RANGE;
D O I:
10.1136/bmjresp-2020-000694
中图分类号:
R56 [呼吸系及胸部疾病];
学科分类号:
摘要:
Introduction Airway clearance techniques (ACTs) are a gold standard of cystic fibrosis management; however, the majority of research evidence for their efficacy is of low standard; often attributed to the lack of sensitivity from outcome measures (OMs) used historically. This randomised controlled trial (RCT) investigates these standard OMs (sputum weight, forced expiratory volume in 1 s) and new OMs (electrical impedance tomography (EIT), multiple breath washout (MBW) and impulse oscillometry (IOS)) to determine the most useful measures of ACT. Methods and analysis This is a single-centre RCT with crossover design. Participants perform MBW, IOS and spirometry, and then are randomised to either rest or supervised ACT lasting 30-60 min. MBW, IOS and spirometry are repeated immediately afterwards. EIT and sputum are collected during rest/ACT. On a separate day, the OMs are performed with the other intervention. Primary endpoint is difference in change in OMs before and after ACT/rest. Sample size was calculated with 80% power and significance of 5% for each OM (target n=64). Ethics and dissemination Ethics approval was gained from the London-Chelsea Research Ethics Committee (reference 16/LO/0995, project ID 154635). Dissemination will involve scientific conference presentation and publication in a peer-reviewed journal.
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页数:8
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